forked from deweylab/RSEM
/
rsem-run-ebseq
executable file
·128 lines (67 loc) · 6.52 KB
/
rsem-run-ebseq
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
117
118
119
120
121
122
123
124
125
126
#!/usr/bin/env perl
use Getopt::Long;
use Pod::Usage;
use FindBin;
use lib $FindBin::RealBin;
use rsem_perl_utils;
use Env qw(@PATH);
@PATH = ("$FindBin::RealBin/EBSeq", @PATH);
use strict;
my $ngvF = "";
my $help = 0;
GetOptions("ngvector=s" => \$ngvF,
"h|help" => \$help) or pod2usage(-exitval => 2, -verbose => 2);
pod2usage(-verbose => 2) if ($help == 1);
pod2usage(-msg => "Invalid number of arguments!", -exitval => 2, -verbose => 2) if (scalar(@ARGV) != 3);
pod2usage(-msg => "ngvector file cannot be named as #! # is reserved for other purpose!", -exitval => 2, -verbose => 2) if ($ngvF eq "#");
my $command = "";
my @conditions = split(/,/, $ARGV[1]);
pod2usage(-msg => "At least 2 conditions are required for differential expression analysis!", -exitval => 2, -verbose => 2) if (scalar(@conditions) < 2);
if ($ngvF eq "") { $ngvF = "#"; }
$" = " ";
$command = "rsem-for-ebseq-find-DE $FindBin::RealBin/EBSeq $ngvF $ARGV[0] $ARGV[2] @conditions";
&runCommand($command)
__END__
=head1 NAME
rsem-run-ebseq - Wrapper for EBSeq to perform differential expression analysis.
=head1 SYNOPSIS
rsem-run-ebseq [options] data_matrix_file conditions output_file
=head1 ARGUMENTS
=over
=item B<data_matrix_file>
This file is a m by n matrix. m is the number of genes/transcripts and n is the number of total samples. Each element in the matrix represents the expected count for a particular gene/transcript in a particular sample. Users can use 'rsem-generate-data-matrix' to generate this file from expression result files.
=item B<conditions>
Comma-separated list of values representing the number of replicates for each condition. For example, "3,3" means the data set contains 2 conditions and each condition has 3 replicates. "2,3,3" means the data set contains 3 conditions, with 2, 3, and 3 replicates for each condition respectively.
=item B<output_file>
Output file name.
=back
=head1 OPTIONS
=over
=item B<--ngvector> <file>
This option provides the grouping information required by EBSeq for isoform-level differential expression analysis. The file can be generated by 'rsem-generate-ngvector'. Turning this option on is highly recommended for isoform-level differential expression analysis. (Default: off)
=item B<-h/--help>
Show help information.
=back
=head1 DESCRIPTION
This program is a wrapper over EBSeq. It performs differential expression analysis and can work on two or more conditions. All genes/transcripts and their associated statistcs are reported in one output file. This program does not control false discovery rate and call differential expressed genes/transcripts. Please use 'rsem-control-fdr' to control false discovery rate after this program is finished.
=head1 OUTPUT
=over
=item B<output_file>
This file reports the calculated statistics for all genes/transcripts. It is written as a matrix with row and column names. The row names are the genes'/transcripts' names. The column names are for the reported statistics.
If there are only 2 different conditions among the samples, four statistics (columns) will be reported for each gene/transcript. They are "PPEE", "PPDE", "PostFC" and "RealFC". "PPEE" is the posterior probability (estimated by EBSeq) that a gene/transcript is equally expressed. "PPDE" is the posterior probability that a gene/transcript is differentially expressed. "PostFC" is the posterior fold change (condition 1 over condition2) for a gene/transcript. It is defined as the ratio between posterior mean expression estimates of the gene/transcript for each condition. "RealFC" is the real fold change (condition 1 over condition2) for a gene/transcript. It is the ratio of the normalized within condition 1 mean count over normalized within condition 2 mean count for the gene/transcript. Fold changes are calculated using EBSeq's 'PostFC' function. The genes/transcripts are reported in descending order of their "PPDE" values.
If there are more than 2 different conditions among the samples, the output format is different. For differential expression analysis with more than 2 conditions, EBSeq will enumerate all possible expression patterns (on which conditions are equally expressed and which conditions are not). Suppose there are k different patterns, the first k columns of the output file give the posterior probability of each expression pattern is true. Patterns are defined in a separate file, 'output_file.pattern'. The k+1 column gives the maximum a posteriori (MAP) expression pattern for each gene/transcript. The k+2 column gives the posterior probability that not all conditions are equally expressed (column name "PPDE"). The genes/transcripts are reported in descending order of their "PPDE" column values. For details on how EBSeq works for more than 2 conditions, please refer to EBSeq's manual.
=item B<output_file.normalized_data_matrix>
This file contains the median normalized version of the input data matrix.
=item B<output_file.pattern>
This file is only generated when there are more than 2 conditions. It defines all possible expression patterns over the conditions using a matrix with names. Each row of the matrix refers to a different expression pattern and each column gives the expression status of a different condition. Two conditions are equally expressed if and only if their statuses are the same.
=item B<output_file.condmeans>
This file is only generated when there are more than 2 conditions. It gives the normalized mean count value for each gene/transcript at each condition. It is formatted as a matrix with names. Each row represents a gene/transcript and each column represent a condition. The order of genes/transcripts is the same as 'output_file'. This file can be used to calculate fold changes between conditions which users are interested in.
=back
=head1 EXAMPLES
1) We're interested in isoform-level differential expression analysis and there are two conditions. Each condition has 5 replicates. We have already collected the data matrix as 'IsoMat.txt' and generated ngvector as 'ngvector.ngvec':
rsem-run-ebseq --ngvector ngvector.ngvec IsoMat.txt 5,5 IsoMat.results
The results will be in 'IsoMat.results' and 'IsoMat.results.normalized_data_matrix' contains the normalized data matrix.
2) We're interested in gene-level analysis and there are 3 conditions. The first condition has 3 replicates and the other two has 4 replicates each. The data matrix is named as 'GeneMat.txt':
rsem-run-ebseq GeneMat.txt 3,4,4 GeneMat.results
Four files, 'GeneMat.results', 'GeneMat.results.normalized_data_matrix', 'GeneMat.results.pattern', and 'GeneMat.results.condmeans', will be generated.
=cut